RESUMEN
To achieve the mission of personalized medicine, centering on delivering the right drug to the right patient at the right dose, therapeutic drug monitoring solutions are necessary. In that regard, wearable biosensing technologies, capable of tracking drug pharmacokinetics in noninvasively retrievable biofluids (e.g., sweat), play a critical role, because they can be deployed at a large scale to monitor the individuals' drug transcourse profiles (semi)continuously and longitudinally. To this end, voltammetry-based sensing modalities are suitable, as in principle they can detect and quantify electroactive drugs on the basis of the target's redox signature. However, the target's redox signature in complex biofluid matrices can be confounded by the immediate biofouling effects and distorted/buried by the interfering voltammetric responses of endogenous electroactive species. Here, we devise a wearable voltammetric sensor development strategy-centering on engineering the molecule-surface interactions-to simultaneously mitigate biofouling and create an "undistorted potential window" within which the target drug's voltammetric response is dominant and interference is eliminated. To inform its clinical utility, our strategy was adopted to track the temporal profile of circulating acetaminophen (a widely used analgesic and antipyretic) in saliva and sweat, using a surface-modified boron-doped diamond sensing interface (cross-validated with laboratory-based assays, R2 â¼ 0.94). Through integration of the engineered sensing interface within a custom-developed smartwatch, and augmentation with a dedicated analytical framework (for redox peak extraction), we realized a wearable solution to seamlessly render drug readouts with minute-level temporal resolution. Leveraging this solution, we demonstrated the pharmacokinetic correlation and significance of sweat readings.
Asunto(s)
Acetaminofén/análisis , Monitoreo de Drogas/métodos , Saliva/química , Sudor/química , Acetaminofén/administración & dosificación , Técnicas Biosensibles/instrumentación , Técnicas Biosensibles/métodos , Monitoreo de Drogas/instrumentación , Humanos , Medicina de Precisión , Dispositivos Electrónicos VestiblesRESUMEN
Through strain-mediated magnetoelectric coupling, it is demonstrated that the magnetocaloric effect of a ferromagnetic shape-memory alloy can be controlled by an electric field. Large hysteresis and the limited operating temperature region are effectively overcome by applying an electric field on a laminate comprising a piezoelectric and the alloy. Accordingly, a model for an active magnetic refrigerator with high efficiency is proposed in principle.
RESUMEN
Cadmium sulfide (CdS) nanoparticles dotted on the surface of multiwalled carbon nanotubes (MWCNTs) have been synthesized by the polyol method. The as-prepared materials were characterized by x-ray powder diffraction, transmission electron microscopy, scanning electron microscopy, and Brunauer-Emmett-Teller adsorption analysis. The results indicate that CdS nanoparticles with diameter of 5-8 nm are thickly and uniformly coated on the surface of the MWCNTs. The photodegradation of azo dye using these materials was evaluated by the degradation of Brilliant Red X-3B under visible light. The coated nanotubes show higher photocatalytic activity than both CdS alone and a CdS/activated carbon sample; in addition, there is an optimum content of MWCNTs. The presence of MWCNTs can also hamper the photocorrosion of CdS. The mechanism for the enhancement of MWCNTs on the adsorption and photocatalytic property of CdS is investigated for the first time.